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Clinical Trial

HIFU for Focal Ablation of Prostate Tissue: An Observational Study

NCT: NCT03620786 · RECRUITING

NCT IDNCT03620786
StatusRECRUITING
Start Date2018-09-26
Completion2028-01-31

Brief Summary

The Sonablate HIFU device was approved by the U.S.FDA for prostate tissue ablation in October, 2015. The purpose of this observational research study is to investigate the localized treatment of prostate cancer using HIFU through clinical data and health-related quality of life (HRQOL) questionnaires.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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